Succinylcholine Chloride
- Product NDC
- 70518-4409
- 11-digit product format
- 705184409
- Labeler code
- 70518
- Product ID
- 70518-4409_3b144826-0fef-8a7c-e063-6394a90ad55b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Succinylcholine Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA211589
- Marketing category
- ANDA
- Marketing start
- 2025-07-29
- Substance
- SUCCINYLCHOLINE CHLORIDE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Depolarizing Neuromuscular Blocker [EPC], Neuromuscular Depolarizing Blockade [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| I9L0DDD30I | SUCCINYLCHOLINE CHLORIDE | 71-27-2 | SUCCINYLCHOLINE CHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4409-0 | 70518440900 | 10 VIAL in 1 CARTON (70518-4409-0) / 10 mL in 1 VIAL (70518-4409-1) | 10 vial | 2025-07-29 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Succinylcholine Chloride | REMEDYREPACK INC. | 2025-07-29 | HUMAN PRESCRIPTION DRUG LABEL | 1 |